Canonical Allele Identifier: CA404877838
Gene: COMP HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.18895728G>T (hg19) chr19:g.18784918G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18784918G>T , CM000681.2:g.18784918G>T GRCh38
NC_000019.9:g.18895728G>T , CM000681.1:g.18895728G>T GRCh37
NC_000019.8:g.18756728G>T NCBI36
NG_007070.1:g.11387C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000222271.7:c.1892C>A MANE Select ENSP00000222271.2:p.Ala631Asp
ENST00000222271.6:c.1892C>A ENSP00000222271.2:p.Ala631Asp
ENST00000425807.1:c.1733C>A ENSP00000403792.1:p.Ala578Asp
ENST00000542601.6:c.1793C>A ENSP00000439156.2:p.Ala598Asp
NM_000095.2:c.1892C>A NP_000086.2:p.Ala631Asp
NM_000095.3:c.1892C>A MANE Select NP_000086.2:p.Ala631Asp
Search 100 bp 5'
Search 100 bp 3'